A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061909



Internal ID19151128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:28081544..28126948hg38UCSC Ensembl
Innerchr21:29453863..29499267hg19UCSC Ensembl
Innerchr21:28375734..28421138hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3845405
hg1945405
hg1845405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600104
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061909
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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